Cystic Fibrosis Foundation - Click here for homepage
This is the official site for Cystic Fibrosis. This page serves as a jump off point to many resources and you can join the foundation on Facebook and on You Tube. This site also has information about clinical trials and pages and articles about children and adults with Cystic Fibrosis.
The photos below are a depiction of Cystic Fibrosis in the 1960's. It makes you realize that there have been many advancements in treatments, research, products, and the prognosis for this disease. Current research has advanced the average life expectancy to 37 years.
Rena's information on Cystic Fibrosis. The following website reveals all sorts of information on cystic fibrosis. They have everything from new related news to picture galleries to nutrition and fitness. You may become a member of this website and then upload information and talk to others, children and adults, that also have cystic fibrosis. It's really great to become a member because you gain access to blogs, forums, and many other networking type options. This website is very user friendly and allows people to interact with others and share wonderful stories and memories. There's also video links that are very informational and fun to watch. There honestly is way too much to write about so just go visit the website! http://www.cysticfibrosis.com/
Joseph Cochran's information on Cystic Fibrosis: Through the Mayo Clinic, you can read the symptoms, signs, things to do, when to seek medical advice, and treatment options. Very informative with links to other pages and articles: http://www.mayoclinic.com/health/cystic-fibrosis/ds00287/dsection
symptoms= This is a news clip about a 37 year old male with Cystic Fibrosis who runs marathons. His determination is very inspiring. http://www.youtube.com/watch?v=csXBIztpKZY. This video submitted by Tammy Guthery.
http://ww.lungusa.org
The American Lung Association gives the statistical information on many lung diseases. Cystic Fibrosis can have many other secondary lung issues that may need to be treated by pulmonologists. This link is a wealth of information on all lung related issues. Web site submitted by Laura Harris
MedicineNet.com http://www.medicinenet.com/cystic_fibrosis/article.htm
This site has a wealth of information. It links to 10 top articles about Cystic Fibrosis and has links to the signs and symptoms of Cystic Fibrosis. The website also has links to picture slideshows, procedures and tests, medications, and a medical term dictionary. Submitted by Anita Robinson
This website is a blog with true stories about people with Cystic Fibrosis and about how families are dealing with the news when a loved one has been diagnosed. Pictures are included with some of the blogs. The stories are heartwarming and uplifting. These are true stories of how families are dealing with Cystic Fibrosis.
Through the Mayo Clinic, you can read the symptoms, signs, things to do, when to seek medical advice, and treatment options. Very informative with links to other pages and articles.
Submitted by; Joseph Cochran
This is a link that will direct you to a 10 minute documentary about a 10 year old girl diagnosed with cystic fibrosis. This project details what it is like to live everyday with cystic fibrosis http://www.youtube.com/watch?v=WUsuGKzdDg8
Sunmitted by Brianna Cantrell
http://www.kidhealth.org/kid/health/_problems/heart/cystic_fibrosis.html
This is a kid friendly site that provides info for kids, parents, and teens.
It provides multiple links: health problems, staying healthy, illnesses & injuries, how the body works, kids talk, staying safe, and much more. This site has lots of info to help kids make connections and have a better understanding of CF so that they can live healthy and have happier lives.
Submitted by Ruby Reasonover
The following is a link to a website that includes a good discussion about signs and syptoms, as well as how it affects the body. http://www.chp.edu/CHP/Cystic+Fibrosis
Submitted by Lisa Kennamer
___ http://www.mycysticfibrosis.com/
This is a sight you can join if you have a family member or friend with Cystic Fibrosis. This is a support group that has newsletters. You can also chat with others that are dealing with Cystic Fibrosis.
Submitted By: Anna McSwain
The March of Dimes is a not-for-profit organization. Our mission is to improve the health of babies by preventing birth defects, premature birth, and infant mortality.
http://www.cff.org/
This is the official site for Cystic Fibrosis. This page serves as a jump off point to many resources and you can join the foundation on Facebook and on You Tube. This site also has information about clinical trials and pages and articles about children and adults with Cystic Fibrosis.
The photos below are a depiction of Cystic Fibrosis in the 1960's. It makes you realize that there have been many advancements in treatments, research, products, and the prognosis for this disease. Current research has advanced the average life expectancy to 37 years.
Rena's information on Cystic Fibrosis. The following website reveals all sorts of information on cystic fibrosis. They have everything from new related news to picture galleries to nutrition and fitness. You may become a member of this website and then upload information and talk to others, children and adults, that also have cystic fibrosis. It's really great to become a member because you gain access to blogs, forums, and many other networking type options. This website is very user friendly and allows people to interact with others and share wonderful stories and memories. There's also video links that are very informational and fun to watch. There honestly is way too much to write about so just go visit the website! http://www.cysticfibrosis.com/
Joseph Cochran's information on Cystic Fibrosis: Through the Mayo Clinic, you can read the symptoms, signs, things to do, when to seek medical advice, and treatment options. Very informative with links to other pages and articles: http://www.mayoclinic.com/health/cystic-fibrosis/ds00287/dsection
symptoms=This is a news clip about a 37 year old male with Cystic Fibrosis who runs marathons. His determination is very inspiring. http://www.youtube.com/watch?v=csXBIztpKZY. This video submitted by Tammy Guthery.
http://ww.lungusa.org
The American Lung Association gives the statistical information on many lung diseases. Cystic Fibrosis can have many other secondary lung issues that may need to be treated by pulmonologists. This link is a wealth of information on all lung related issues. Web site submitted by Laura Harris
MedicineNet.com
http://www.medicinenet.com/cystic_fibrosis/article.htm
This site has a wealth of information. It links to 10 top articles about Cystic Fibrosis and has links to the signs and symptoms of Cystic Fibrosis. The website also has links to picture slideshows, procedures and tests, medications, and a medical term dictionary. Submitted by Anita Robinson
http://en.wordpress.com/tag/cystic-fibrosis/
This website is a blog with true stories about people with Cystic Fibrosis and about how families are dealing with the news when a loved one has been diagnosed. Pictures are included with some of the blogs. The stories are heartwarming and uplifting. These are true stories of how families are dealing with Cystic Fibrosis.
Submitted by: Susan Riggs
http://www.mayoclinic.com/cystic-fibrosis/ds00287/dsection=symptoms
Through the Mayo Clinic, you can read the symptoms, signs, things to do, when to seek medical advice, and treatment options. Very informative with links to other pages and articles.
Submitted by; Joseph Cochran
This is a link that will direct you to a 10 minute documentary about a 10 year old girl diagnosed with cystic fibrosis. This project details what it is like to live everyday with cystic fibrosis
http://www.youtube.com/watch?v=WUsuGKzdDg8
Sunmitted by Brianna Cantrell
http://www.kidhealth.org/kid/health/_problems/heart/cystic_fibrosis.html
This is a kid friendly site that provides info for kids, parents, and teens.
It provides multiple links: health problems, staying healthy, illnesses & injuries, how the body works, kids talk, staying safe, and much more. This site has lots of info to help kids make connections and have a better understanding of CF so that they can live healthy and have happier lives.
Submitted by Ruby Reasonover
The following is a link to a website that includes a good discussion about signs and syptoms, as well as how it affects the body.
http://www.chp.edu/CHP/Cystic+Fibrosis
Submitted by Lisa Kennamer
___
http://www.mycysticfibrosis.com/
This is a sight you can join if you have a family member or friend with Cystic Fibrosis. This is a support group that has newsletters. You can also chat with others that are dealing with Cystic Fibrosis.
Submitted By: Anna McSwain
http://www.marchofdimes.com/pnhec/4439_1213.asp
The March of Dimes is a not-for-profit organization. Our mission is to improve the health of babies by preventing birth defects, premature birth, and infant mortality.
Submitted by Karen Gallian
http://cysticfibrosis.about.com/od/symptoms/u/symptomsanddiagnosis.htm
This site discusses the symptoms, diagnosis, and treatments of Cystic Fibrosis (CF). It also provides great insight on living with CFSubmitted by Cathy Brown
http://www.famouspeoplebiography411.com/Famous-people/Famous-People-With-Cystic-Fibrosis.html
This site gives a brief overview of the symptoms of this disease. It lists well known people from the past and present that accomplished great things while living with cystic fibrosis. Submitted by Deb Talley.
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